ABCB4 Mutations in Adults Cause a Spectrum Cholestatic Disorder Histologically Distinct from Other Biliary Disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology,Physiology
Link
https://link.springer.com/content/pdf/10.1007/s10620-022-07416-9.pdf
Reference21 articles.
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2. Vitale G, Gitto S, Raimondi F, Mattiaccio A et al. Cryptogenic cholestasis in young and adults: ATP8B1, ABCB11, ABCB4, and TJP2 gene variants analysis by high-throughput sequencing. J Gastroenterol 2018;53:945–958.
3. Miller GC, Clouston AD. Adult onset of genetic disorders in bile acid transport in the liver. Hum Pathol 2020;96:2–7.
4. Ziol M, Barbu V, Rosmorduc O, Frassati-Biaggi A et al. ABCB4 heterozygous gene mutations associated with fibrosing cholestatic liver disease in adults. Gastroenterology 2008;135:131–141.
5. Ovadia C, Seed PT, Sklavounos A, Geenes V et al. Association of adverse perinatal outcomes of intrahepatic cholestasis of pregnancy with biochemical markers: results of aggregate and individual patient data meta-analyses. Lancet 2019;393:899–909.
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